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Neo Medical Cage kit

FDA UDI

Class II (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Medical Cage kit FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
Cage anatomical curved 32mm, 7 mm, 5 ° FDA UDI
Model / Reference
AC-32-07-05 FDA UDI
Description
Cage anatomical curved 32mm, 7 mm, 5 ° FDA UDI

Identifiers

Catalog Number
AC-32-07-05 FDA UDI
Primary DI / UDI-DI
07640177822499 FDA UDI
510(k) Number
K191796 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Height — 7 Millimeter FDA UDI
Length — 32 Millimeter FDA UDI

Category: Metallic spinal interbody fusion cage

Neo Medical Cage kit by Neo Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neo Medical Inc.

Sources (1)

  • FDA UDI 11e5026f-6ecd-4d57-bc45-9bae2d1231dd 37 fields · synced Jun 7, 2026